Soak and coke

ABSTRACT

There is provided herein a method for producing hydrogen gas, comprising: sorbing a liquid hydrocarbon fuel to a gasification catalyst to form a sorbed hydrocarbon fuel; heating said sorbed hydrocarbon fuel to a first temperature for a first period of time sufficient to form coke; and gasifying said coke at a second temperature at a pressure for a second period of time in the presence of water and/or oxygen, so as to produce hydrogen gas and carbon monoxide and to regenerate said catalyst. In particular, the hydrocarbon fuel can be a liquid biomass, such pyrolysis oil, and the method can be CO 2  neutral.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Continuation Application which claims the benefitof and priority to U.S. Non-Provisional application Ser. No. 13/357,989filed Jan. 25, 2012, entitled “Soak and Coke,” which is herebyincorporated by reference in its entirety.

FEDERALLY SPONSORED RESEARCH STATEMENT

Not applicable.

FIELD OF THE INVENTION

The invention relates to hydrogen production, particularly from ahydrocarbon fuel using a catalyst.

BACKGROUND OF THE INVENTION

Hydrogen generation and availability are perennial issues for oilrefiners. Steam methane reforming (SMR) is the option of choice formany, but only at the expense of significant CO₂ emissions, which may belimited by future regulations and carbon taxes. Biomass-derived hydrogencan help alleviate and/or compliment the hydrogen supply of refineryoperation, while simultaneously reducing the carbon footprint and, thus,lowering cost associated with pollution and greenhouse gas emission.

CN 1435369 describes a method for preparing hydrogen gas by catalyticcracking of a biomass, comprising introducing heated air tofluidized-bed reactor, burning biomass in the presence of steam,fluidizing the biomass, gasifying, and cracking to generate ahydrogen-enriched gas.

CN 1214972 describes gasification of a solid biomass in a down draftgasification reactor. The resulting gas undergoes a steam methanereforming and a tar fission reaction, producing a hydrogen-rich gas.

U.S. 2008244976 describes a method and system for gasifying biomass inan indirectly heated gasifier, and provides a method to eliminatecondensable organic material from the resulting product gas. The methodcomprises a tar removal step that uses a circulating catalyst to crackorganics and produce additional gas. The catalyst is heated in thegasification reactor and transferred to a conditioning chamber, where itcatalyzes the cracking step.

U.S. 2007100003 describes a hybrid system for biomass gasification,wherein the biomass is pyrolyzed and the resulting solids and vapors areprocessed through supercritical steam gasification. Product gases arepurified in an amine wash scrubber, an adiabatic pre-reformer breaksdown remaining aromatic compounds, and are steam-reformed.

What is lacking is a simple and more efficient method to producehydrogen without significant increase in CO₂ levels. We describe amethod to adsorb biomass onto a catalyst, followed by gasification toproduce H₂ and regenerate the catalyst.

SUMMARY OF THE INVENTION

We describe herein a method to adsorb biomass onto a catalyst, followedby gasification to produce H₂ and regenerate the catalyst. In preferredembodiments, the method is carbon neutral.

A biomass starting material, for example a pyrolysis oil, can beintroduced and adsorbed onto a gasification catalyst, for examplenickel, supported nickel, or other metal. Adsorption occurs underambient conditions without additional heating, thus saving operatingcost in energy savings and consequently also reducing CO₂ emissions. The“soaked” catalyst is then introduced to a reactor hot zone where cokingoccurs. Gasification, for example steam gasification, both regeneratesthe catalyst and produces bio-syngas, a combination of hydrogen andcarbon monoxide. The bio-syngas can further undergo a water gas shift(WGS) reaction, yielding hydrogen and so-called “bio-CO₂”, which isregarded as carbon neutral. Because of the catalyst, lower temperaturecan be used for the reaction, improving the economy of the process.

Soaking provides the biomass time to adsorb to the catalyst instead ofelsewhere in a reactor, where it would cause fouling. Soaking alsoreduces or prevents equipment downtime and ensures that potentialcatalyst poisons contained in the biomass starting material are retainedin the first part of the process and do not elaborate downstream. Thus,soaking produces gases that require less purification and clean-up thanprevious methods. When a supported catalyst is used, the catalyst, oncefluidized, can act as an abrasive to keep the reactor from fouling.

Specifically, this application provides a method for producing hydrogengas, comprising: sorbing a liquid hydrocarbon fuel to a gasificationcatalyst to form a sorbed hydrocarbon fuel; heating said sorbedhydrocarbon fuel to a first temperature for a first period of timesufficient to form coke; and gasifying said coke at a second temperaturefor a second period of time in the presence of water and/or oxygen, soas to produce a gasesous mixture comprising hydrogen gas and carbonmonoxide, and to regenerate said catalyst.

The catalyst can be any catalyst that is known to decompose/crackorganic molecules. Preferably, the catalyst is provided on a solidsupport, such as dolomite, silicas, aluminas, clays, etc., and mixturesthereof.

The water can be introduced into the reaction in the form of steam. Themethod can further comprise separating said hydrogen gas from saidcarbon monoxide. The method can further comprise subjecting said gaseousmixture to a water-gas shift, as to produce additional hydrogen gas andcarbon dioxide; and separating said hydrogen gas and said additionalhydrogen gas from said carbon dioxide and gaseous mixture.

The first period of time can depend on the temperature used: the lowerthe temperature, the longer the time required. For example, lowertemperatures require between 10 minutes to more than 2 hours whilehigher temperatures require contact times of less than 10 minutes toform coke on said catalyst. It is particularly advantageous when themethod uses a liquid biomass, such as a pyrolysis oil.

In a particular embodiment, there is provided a method for producinghydrogen gas, comprising: sorbing a liquid or liquefied biomass to agasification catalyst to form a sorbed biomass, wherein saidgasification catalyst comprises one or more selected from the groupconsisting of nickel, palladium, platinum, iron, cobalt, manganese,tungsten, molybdenum, tantalum, alkali earth metals, alkali earth metaloxides, dolomite, sand, and mixtures thereof; amd heating said liquidbiomass to 50° C.-650° C. for a first period of time sufficient to formcoke; and gasifying said coke at 400° C.-1000° C. in the presence ofsteam and/or oxygen and said catalyst, so as to produce a gaseousmixture comprising hydrogen gas and carbon monoxide, and to regeneratesaid catalyst.

DESCRIPTION OF EMBODIMENTS OF THE INVENTION

The following abbreviations are used herein:

MS Mass spectrometry SMR Steam methane reforming TGA Thermogravimetricanalysis WGS Water gas shift

“Hydrocarbon fuel” refers to any fuel, including fossil fuels, biomassfuels, and the like. “Fossil fuel” refers to fuel formed from naturalresources, such as anaerobic decomposition of organisms, for examplephytoplankton, zooplankton, and plant matter. Fossil fuels can includecoal, crude oil, and natural gas.

“Biomass” refers to any biological material from living, or recentlyliving organisms, such as wood, paper, agricultural waste, consumerwaste, wood and paper waste, cereal and grass crops, vegetable and treeoils, algae, and the like. “Biomass fuel” or “biofuel” refers to a fuelderived from biological material of living or recently living organisms.Examples of biomass fuel include wood, charcoal, hydrogen gas, alcohol(e.g., ethanol), organic oils (e.g., palm oil, rapseed, jathorpa),manure, grass cuttings, and biodiesel. Sources of biological materialsused in biomass fuel include, but are not limited to trees (e.g.,poplar, pine, willow, oak, maple, eucalyptus, oil palm), miscanthus,switchgrass, hemp, corn, cassava, sorghum, sugarcane, sugar beet,soybean, sunflower, wheat, rapeseed, jathorpa, salicornia, mahua,mustard, flax, field pennycress, pongamia pinnata, and algae.

The liquid hydrocarbon fuel can be a liquid biomass, for examplepyrolysis oil. “Pyrolysis oil” or “bio-oil” refers to a synthetic fueldesigned to substitute petroleum. It is typically extracted by abiomass-to-liquid technology, using destructive distillation from driedbiomass in a reactor at about 500° C. followed by cooling. Althoughexact composition of a pyrolysis oil depends on the biomass sources andprocessing conditions, a typical composition is shown in Table 1. Theoil is acidic, has a density of about 1.2-1.3 kg/L, and an oxygencontent to 40-50%, mostly from water. The heating value is about 16-21MJ/kg, with a flash point of 40-100° C. Pyrolysis oil is denser thandiesel, typically cannot be blended with diesel, and is notauto-igniting in a diesel engine.

TABLE 1 Typical pyrolysis oil content Component Percent weight ofcomposition Water 20-28% Suspended solids and pyrolytic lignin 22-36%Hydroxyacetaldehyde 8-12% Levoglucosan 3-8% Acetic acid 4-8% Acetol 3-6%Cellubiosan 1-2% Glyoxal 1-2% Formaldehyde 3-4% Formic acid 3-6%

“Sorption” refers to any action of absorption into or adsorption onto asolid material through chemical (chemisorption) and/or physical(physiorption) interactions.

“Coke” refers to solid carbonaceous material derived fromcarbon-containing fuel, such as a hydrocarbon fuel. Coal, for example,produces coke from destructive distillation of low-ash, low-sulfurbituminous coal. Coke derived from petroleum is referred to as“petroleum coke” or “pet coke” or “petcoke”, for example carbonaceoussolid derived from oil refinery coker units or other cracking processes,or hard carbon and other crude oil impurities formed on the insidefurnace tubes. Coke has several industrial uses, including, but notlimited to, making electrodes for aluminum manufacturing, fuel, andsteel manufacture.

“Coking” refers to a process of forming coke from a carbon-containingcombustible starting material. For example, a starting material can beheated from about 100° C. to about 450° C., wherein lower molecularweight chemicals are distilled off and coke is left behind. Coking canbe used to improve hydrocarbon liquids for further upgrading bycatalytic processing because many chemicals that poison catalysts havebeen removed. Removal of heteroatoms from the starting material iscounterbalanced by increased hydrogen content in the supernatant,because most polynuclear aromatic building blocks in the petroleumcontain heteroatoms that reactively separate into the coke.

“Gasification” refers to conversion of a hydrocarbon fuel, such as coal,petroleum, biofuel, biomass, or coke derived from a variety of sources,into carbon monoxide (CO) and hydrogen (H₂) by reacting the fuel atelevated temperature (>700° C.) with oxygen and/or steam and producingsyngas. Gasification can use materials that are not otherwise usefulfuels, such as biomass or organic waste. In addition, high-temperaturecombustion refines out corrosive ash element, such as chlorine andpotassium, producing clean gas from otherwise problematic fuels.

“Steam methane reforming”, “steam reforming” or “SMR” refers to a commonand relatively inexpensive gasification process for producing bulkhydrogen. At temperatures of 700-1100° C. in the presence of ametal-based catalyst (e.g., nickel), steam endothermically reacts withmethane to yield carbon monoxide and hydrogen (Equation 1):

CH₄+H₂O⇄CO+3H₂  (Equation 1)

Additional hydrogen can be recovered by a lower-temperature, exothermicreaction with the carbon monoxide produced (Equation 2):

CO(g)+H₂O(g)⇄CO₂(g)+H₂(g)  (Equation 2)

This reversible, gas-phase reaction, known as the water gas shift (WGS),can quickly equilibrate at gasifer temperatures, balancing theconcentrations of CO, H₂O, CO₂ and H₂.

The gasification catalyst can comprise, for example, nickel, palladium,platinum, iron, cobalt, manganese, tungsten, molybdenum, tantalum,alkali earth metals, alkali earth metal oxides, sand, dolomite, andmixtures thereof. Alkali earth metals consist of beryllium, magnesium,calcium, strontium, barium, and radium. Examples of alkali earth metaloxides include, but are not limited to beryllia (beryllium oxide, BeO),magnesia (magnesium oxide, MgO), lime (calcium oxide, CaO), strontia(strontium oxide, SrO), and baryta (barium oxide, BaO).

Small particle size with high surface area is preferred for catalysts.The bulk density ranges from 0.5 to 1.2 g/mL, preferably between 0.5 to0.9 g/mL, and having a particle size distribution ranging from 10 to 150μm, preferably between 50 to 100 μm. The first temperature can be from50° C. to 650° C., preferably between 70° C. to 400° C., and mostpreferably between 80° C. to 300° C. The first period of time can befrom less than 60 seconds to 2 hours, preferably between 60 seconds to 1hour, most preferably between 1 and 10 minutes.

A “gasifier” is a device in which a hydrocarbon fuel undergoespyrolysis, combustion and, ultimately, gasification. Pyrolysis occurswhen a carbon-containing material, such as a hydrocarbon fuel, isheated. Volatiles are released and char is produced, resulting in forexample a 70% weight loss. The structure and composition of the charvaries depending on the property of the fuel. Combustion occurs as thevolatile products and some of the char reacts with oxygen to form CO₂and CO, providing heat for the subsequent gasification. Types ofgasifiers include, for example, counter-current fixed bed; co-currentfixed bed, fluidized bed, and entrained flow gasifiers.

The counter-current fixed bed (“up draft”) gasifier comprises a fixedbed of hydrocarbon fuel through which steam, oxygen and/or air flow incounter-current configuration. Ash is removed dry or as a slag. Becausethis gasifier uses a fixed bed of fuel, the fuel must have a highmechanical strength and is ideally non-caking so that the bed can bepermeable. Thermal efficiency is high because gas exit temperatures arerelatively low, but tar and methane production is significant at typicaloperation temperatures, so product gas must be extensively cleanedbefore use.

The co-current fixed bed (“down draft”) gasifier is similar to thecounter-current type, but the steam, oxygen and/or air flow inco-current configuration with the fuel downwards. Heat is added to theupper part of the bed, either by combusting small amounts of the fuel orfrom external heat sources. Since tar must pass through a hot bed ofchar in this configuration, tar levels are much lower than thecounter-current type.

In the fluidized bed reactor, the fuel is fluidized in oxygen, steamand/or air. The ash is removed dry or as heavy precipitants. Thetemperatures are relatively low in dry ash gasifiers, so the fuel mustbe highly reactive. The agglomerating gasifiers have slightly highertemperatures, and are suitable for higher rank coals. Fuel throughput ishigher than for the fixed bed, but not as high as for the entrained flowgasifier. Fluidized bed gasifiers are most useful for fuels, such asbiofuels, that form ash that is highly corrosive to the walls ofslagging gasifiers.

In the entrained flow gasifier, a dry pulverized solid, an atomizedliquid fuel or fuel slurry is gasified with oxygen or, less frequently,air in a co-current flow. Gasification occurs in a dense cloud of veryfine particles at high temperature and pressure. The high temperatureand pressure allows higher throughput and produces less tar and methanethan other gasifiers, but the oxygen requirement is higher. Entrainedflow gasifiers remove most ash as a slag as the operating temperature iswell above the ash fusion temperature. Some fuels, in particular certaintypes of biomasses, can form slag that is corrosive for protectiveceramic inner walls.

The second temperature can be 400° C.-1000° C. The second period timecan depend on the temperature used: the lower the temperature, thelonger the time required. For example, low temperatures require between10 minutes to more than 2 hours while high temperatures require contacttimes of less than 10 minutes. The pressure can be above ambientpressure, for example between 14 psi and 300 psi (about 100 kPa to 2MPa).

“Synthesis gas” or “syngas” refers to a gas consisting essentially of H₂and CO, which can be produced from a hydrocarbon fuel, such as a biomassfuel. Syngas derived from a biomass can be referred to as “biosyngas”.Hydrogen can be recovered from syngas. Syngas can also be catalyticallyconverted to methanol, run through a biological reactor to produceethanol, or be converted using a Fischer-Tropsch catalyst into a liquidstream with properties similar to diesel fuel, called Fischer-Tropschdiesel. These processes, however, can be expensive, and can generatefuels that are not easily assimilated in current transportationtechnology. Nonetheless, using syngas is potentially more efficient thandirect combustion of the original fuel, because it can be combusted athigher temperatures or in fuel cells, so that the thermodynamic upperlimit to the efficiency defined by Carrot's rule is higher or notapplicable.

“Thermogravimetric analysis” or “TGA” refers to a method for determiningchanges in sample weight as a function of temperature. The analysisrelies on highly precise measurements of weight, temperature andtemperature change. A derivative weight loss curve can tell the point atwhich weight loss is most apparent. Interpretation can be limitedwithout further modification and deconvolution of overlapping peaks. TGAcan be used in tandem with mass spectrometry (MS) to determine off-gascomposition.

The present invention is exemplified with respect to gasification of abiomass feedstock. However, this feedstock is exemplary only, and theinvention can be broadly applied to any hydrocarbon fuel, includingfossil fuels such as crude oil and coal. The following examples areintended to be illustrative only, and not unduly limit the scope of theappended claims.

EXAMPLE 1 Soaking and Coking of Pyrolysis Oil

A neat pyrolysis oil was soaked onto various supports including silicaand nickel supported on silica. Using incipient wetness, the ratio ofpyrolysis oil/support reached 3:1. The soaked material was placed in aflask and heated to temperatures up to 500° C. in an inert atmosphere.

Water vapor was condensed downstream. Remaining off-gases were analyzedby online mass spectrometry (MS). Additionally, fresh and resultingcoked support was analyzed using thermogravimetric analysis massspectroscopy (TGA-MS). Used, neat pyrolysis oil coked completely between320° C. and 350° C., where complete coking was defined as the point whenno CO₂ evolution could be monitored. The nickel-containing catalystlowered coking temperatures by 50° C.-100° C. Furthermore, off-gascomposition changed significantly when using the nickel-based catalyst:more light carbon-containing gases (e.g., methane, ethane) were observedcompared to use of unmodified silica. Therefore, the soak and cokemethod was more efficient and produced a better product.

The use of the word “a” or “an” when used in conjunction with the term“comprising” in the claims or the specification means one or more thanone, unless the context dictates otherwise.

The term “about” means the stated value plus or minus the margin oferror of measurement or plus or minus 10% if no method of measurement isindicated.

The use of the term “or” in the claims is used to mean “and/or” unlessexplicitly indicated to refer to alternatives only or if thealternatives are mutually exclusive.

The terms “comprise”, “have”, “include” and “contain” (and theirvariants) are open-ended linking verbs and allow the addition of otherelements when used in a claim.

The following references are incorporated by reference in theirentirety:

CN 1435369.

CN 1214972.

U.S. 2008244976.

U.S. 2007100003.

1. A method for producing hydrogen gas, comprising: a. sorbing a liquidhydrocarbon fuel to a gasification catalyst to form a sorbed hydrocarbonfuel; b. heating said sorbed hydrocarbon fuel to a first temperaturefrom about 50° C.-650° C. for a first period of time sufficient to formcoke; and c. gasifying said coke at a second temperature at a pressurefor a second period of time in the presence of water and/or oxygen, soas to produce a gaseous mixture comprising hydrogen gas and carbonmonoxide, and to regenerate said catalyst, wherein said liquidhydrocarbon fuel is a liquid biomass or a liquefied biomass. 2.(canceled)
 3. The method of claim 1, wherein said liquid hydrocarbonfuel is pyrolysis oil.
 4. The method of claim 1, wherein saidgasification catalyst comprises one or more selected from the groupconsisting of nickel, palladium, platinum, iron, cobalt, manganese,tungsten, molybdenum, tantalum, alkali earth metals, and oxides thereof,dolomite, sand, and mixtures thereof.
 5. The method of claim 1, whereinsaid gasification catalyst has a particle size distribution of 10 μm to150 μm.
 6. The method of claim 5, wherein said particle sizedistribution is 50 μm to 100 μm.
 7. (canceled)
 8. The method of claim 8,wherein said first temperature is 70° C.-400° C.
 9. The method of claim9, wherein said first temperature is 80° C.-300° C.
 10. The method ofclaim 1, wherein said first period of time is 1 second to 2 hours. 11.The method of claim 10, wherein the first period of time is 1-60minutes.
 12. The method of claim 11, wherein the first period of time is1-10 minutes.
 13. The method of claim 1, wherein said second temperatureis from 400° C. to 1000° C.
 14. The method of claim 1, furthercomprising: a. subjecting said gaseous mixture to a water-gas shift, asto produce additional hydrogen gas; and b. isolating said hydrogen gasand said additional hydrogen gas from said gaseous mixture.
 15. A methodfor producing hydrogen gas, comprising: a. sorbing a liquid or liquefiedbiomass to a gasification catalyst to form a sorbed biomass, whereinsaid gasification catalyst comprises one or more selected from the groupconsisting of nickel, palladium, platinum, iron, cobalt, manganese,tungsten, molybdenum, tantalum, alkali earth metals, and oxides thereof,dolomite, sand, and mixtures thereof; b. heating said sorbed biomass toa first temperature of 50° C.-650° C. for a first period of time of 1second to 2 hours to produce coke; and c. gasifying said coke at asecond temperature 400° C.-1000° C. in the presence of steam and/oroxygen and said catalyst sufficient, so as to produce a gaseous mixturecomprising hydrogen gas and carbon monoxide, and to regenerate saidcatalyst.
 16. The method of claim 15, wherein said liquid biomass is apyrolysis oil.
 17. The method of claim 15, wherein said gasificationcatalyst has a particle size distribution of 50 to 100 μm.
 18. Themethod of claim 15, wherein said first period of time is 1-10 minutes.19. The method of claim 15, further comprising: a. subjecting saidgaseous mixture to a water-gas shift, as to produce additional hydrogengas; and b. isolating said hydrogen gas and said additional hydrogen gasfrom said gaseous mixture.
 20. The method of claim 19, wherein saidmethod is carbon neutral.